Results 51 to 60 of about 25,995 (235)

Heterostructured Fe@C/polythiophene metamaterials for compatible ultra-broadband microwave absorption and low infrared emissivity

open access: yesNano Research
Achieving spectral compatibility between microwave absorption (MA) and low infrared emissivity presents a formidable challenge due to the conflicting electromagnetic requirements of different bands. Herein, we engineered a gradient metamaterial utilizing
Yi Liu   +9 more
doaj   +1 more source

Biomass DNA: An Emerging Building Block for Advanced Materials

open access: yesAdvanced Materials, EarlyView.
Biomass DNA is rapidly emerging from its traditional role as a genetic blueprint to serve as a versatile abundant, highly programmable polymeric building block. This review highlights the transformation of macroscopic bulk biomass DNA into next generation of functional materials, spanning from dynamic hydrogels, sustainable bioplastics, and high ...
Yuwei Hu, Itamar Willner, Li Niu
wiley   +1 more source

Polythiophene-Encapsulated Bimetallic Au-Fe3O4 Nano-Hybrid Materials: A Potential Tandem Photocatalytic System for Nondirected C(sp2)–H Activation for the Synthesis of Quinoline Carboxylates

open access: yes, 2017
Hetero-oligophenylene derivative 3 appended with thiophene moieties has been designed and synthesized which undergoes aggregation to form J-type fluorescent aggregates in in H2O/THF (7/3) media.
Subhamay Pramanik   +11 more
core   +1 more source

Electrochemical Generation and Spectroscopic Characterization of Charge Carriers within Isolated Planar Polythiophene

open access: yes, 2016
In order to unveil the nature of charge carriers in a doped polythiophene, a sterically isolated polythiophenene, poly­(1EDOT), was electrochemically synthesized on electrodes.
Takeshi Yasuda (1398376)   +4 more
core   +4 more sources

Enzymatic Formation of Polyaniline, Polypyrrole, and Polythiophene Nanoparticles with Embedded Glucose Oxidase

open access: yesNanomaterials, 2019
Polyaniline (PANI), polypyrrole (Ppy), and polythiophene (PTh) composite nanoparticles with embedded glucose oxidase (GOx) were formed by enzymatic polymerization of corresponding monomers (aniline, pyrrole, and thiophene).
Natalija German   +3 more
doaj   +1 more source

Poly(3‐alkylthiophene) Films as Solvent‐Processable Photoelectrocatalysts for Efficient Oxygen Reduction to Hydrogen Peroxide

open access: yesAdvanced Energy & Sustainability Research, 2021
Poly(3‐alkylthiophene) films play a central role in various organic devices due to their solvent processability and their remarkable electrical and optical properties.
Kouki Oka   +3 more
doaj   +1 more source

Dicationic Ion‐Pair Doping Enables Stable and High‐Performing Conducting Polymers for Organic Thermoelectrics

open access: yesAdvanced Science, EarlyView.
TAB–2TFSI enables efficient ion‐pair doping across a wide range of conjugated polymers, where the strongly oxidizing TAB core drives charge transfer, and the TFSI counterions promote favorable ionic compensation. This dicationic dopant promotes uniform dopant distribution, improves structural order, and increases carrier delocalization, establishing a ...
Juhyung Park   +14 more
wiley   +1 more source

Electrochromic Properties of Polythiophene Polyrotaxane Film

open access: yes, 2016
The electrochromic properties of a polythiophene polyrotaxane film consisting of a polythiophene backbone wrapped by the tetra-cationic cyclophane, cyclobis(paraquat-p-phenylene), were characterized.
Taichi Ikeda (1687402)   +1 more
core   +1 more source

Achieving 16% Efficiency for Polythiophene Organic Solar Cells with a Cyano‐Substituted Polythiophene

open access: yesAdvanced Functional Materials, 2022
AbstractPolythiophenes (PTs) are promising electron donors in organic solar cells (OSCs) due to their simple structures and excellent synthetic scalability. However, the device performance of PT‐based OSCs is rather poor due mainly to large photon energy losses and an unfavorable active layer morphology.
Xiyue Yuan   +9 more
openaire   +2 more sources

Crystal structure of N-(4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl)-2-(thiophen-3-yl)acetamide

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2017
The title compound, C9H8N2O2S3, crystallizes with two molecules (A and B) in the asymmetric unit. Both have similar conformations (overlay r.m.s. deviation = 0.209 Å) and are linked by an N—H...O hydrogen bond. In both molecules, the thiophene rings show
Trung Vu Quoc   +4 more
doaj   +1 more source

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